Established in 1998 InClin is a full service Contract Research Organization with offices in the San Francisco Bay Area and Sydney, Australia. We are a single source provider of an integrated full suite of clinical development services from Phase 1 through Phase 4, including project management, clinical monitoring, site and contract management, vendor management, data management, biostatistics, programming, drug safety, medical monitoring, medical writing, QA inspection readiness, as well as strategic consulting services. Our trials are completed on-time, on-budget, with personalized, high quality service. >150 Sponsor companies >400 trials >100 pivotal Phase 2 and Phase 3 studies 9 NDAs, 1 sNDA, and 2 BLAs Our staff has an average of 20+ years of clinical research experience. Our employee retention rate is high, so the InClin team that initiates your trial will be the same team that completes it. With broad multidisciplinary training, the senior management team of InClin has the insight, integrity and ingenuity to assist its clients in the design and execution of sound clinical programs. The InClin difference is in our people and clinical teams who serve sponsors on a daily basis. We understand the solid partnerships are the foundation of every successful trial. InClin employs senior level clinical research experts that have a passion to work in the drug development industry and care about the success of our sponsors assets. We invest in our employees through training and development and provide tools that best enable them to operationalize efficient clinical trials on time with quality deliverables. InClin manages a rigorous Quality Assurance framework to ensure full compliance with FDA and EMA regulations. We emphasize proactive and transparent communication between the operations team and our sponsors so everyone is confident the study is on plan and on budget throughout the development timeline.